H2S信号在拟南芥响应SO2胁迫过程中的作用

以拟南芥为实验材料,研究植物对H₂S和SO₂处理的转录响应及其关系,并利用外源喷施H₂S及其清除剂的方法,检测SO₂熏气后植株体内H₂S的产生及其生理效应,探讨气体信号分子H₂S在植物响应SO₂胁迫过程中的作用.高通量测序结果发现,H₂S和SO₂处理诱导拟南芥植株多个基因转录水平改变,并有1220个基因在两种处理条件下均差异表达,其中包括多个硫代谢和谷胱甘肽代谢相关基因,表明H₂S和SO₂在调控硫代谢途径中具有交互作用.SO₂熏气诱导拟南芥植株体内H₂S合成酶基因LCD和DES1转录水平提高,胞内H₂S含量增多.同时,超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性升高,含硫抗氧化物谷胱甘肽(GSH)含量及其相关酶谷胱甘肽硫转移酶(GST)和谷胱甘肽过氧化物酶(GPX)活性提高,活性氧H₂O₂含量增加,膜脂过氧化产物丙二醛(MDA)含量与对照相比无显著差异.外源喷施H₂S可进一步提高SO₂熏气下拟南芥植株GSH含量及其相关防御酶的活性,H₂O₂含量降低.但喷施亚牛磺酸(HT)清除H₂S后,SO₂熏气拟南芥植株GSH含量、抗氧化酶SOD、CAT和GST活性降低,MDA含量大幅增加.结果表明,SO₂熏气诱导产生的H₂S可作为信号分子,提高机体抗氧化防御能力,增强植物对SO₂胁迫的抗性.     

Long-term impacts of graphene oxide and Ag nanoparticles on anammox process: Performance, microbial community and toxic mechanism

The increasing application of engineered nanoparticles (NPs) has posed an emerging challenge to constructed wetland wastewater treatment. The performance, microbial community and toxic mechanism of anammox-based unplanted subsurface-flow constructed wetlands (USFCWs) were investigated under the long-term exposure of different graphene oxides (GOs) and Ag NP concentrations. Results showed that the addition of GO could promote TN removal, manifesting as function anammox bacteria C. Anammoxoglobus having a relative high abundance, for GO did not cause significant damage to the cell integrity though there was an increase in ROS concentrations. TN removal would not be obviously affected under exposure of 1?mg/L Ag NPs, for the function gene related to cell biogenesis and repair was up-regulated; while the addition of 10?mg/L Ag NPs would have an inhibiting effect on TN removal in the USFCWs, for the disappearance of some species having anammox ability. Key enzymes of anammox process (NIR and HDH) decreased to some extent under GO and Ag NP exposure, and function gene of defense mechanisms had an increase trend in samples.     

Nitrogen-cycling microbial community functional potential and enzyme activities in cultured biofilms with response to inorganic nitrogen availability

Biofilms mediate crucial biochemical processes in aquatic ecosystems. It was hypothesized that eutrophication may promote the growth of biofilms, resulting in larger numbers of functional genes. However, the metabolic activity and the roles of biofilms in N cycling will be affected by ambient inorganic nitrogen availability, not by the abundance of functional genes. Biofilms were cultured either with replete inorganic nitrogen(N-rep) or without exogenous inorganic nitrogen supply(N-def) in a flow incubator, and the N-cycling gene abundances(nifH, N_2 fixation; amoA, ammonia oxidation, archaea and bacteria; nirS and nirK, denitrification) and enzyme activities(nitrogenase and nitrate reductase) were analyzed. The results showed that, comparing the N-def and N-rep biofilms, the former contained lower nifH gene abundance, but higher nitrogenase activity(NA), while the latter contained higher nifH gene abundance, but lower NA. Different patterns of NA diel variations corresponded to the dynamic microbial community composition and different stages of biofilm colonization. Ammonia oxidizing bacteria(AOB), detected only in N-def biofilms, were responsible for nitrification in biofilms. N-rep biofilms contained high nirS and nirK gene abundance and high denitrification enzyme activity, but N-def biofilms contained significantly lower denitrification gene abundance and activity. In general,the strong N_2 fixation in N-def biofilms and strong denitrification in N-rep biofilms assured the balance of aquatic ecosystems. The results suggested that evaluation of the functional processes of N cycling should not only focus on genetic potential, but also on the physiological activity of biofilms.     

磺胺类兽药对土壤酶活性的影响

采用室内培养的方法,研究磺胺类兽药（磺胺二甲基嘧啶、磺胺甲唑）污染对土壤蔗糖酶、硝酸还原酶、过氧化氢酶、磷酸酶、脲酶和多酚氧化酶活性的影响。结果表明,磺胺类兽药可显著抑制土壤蔗糖酶的活性,其抑制率可达50%以上。兽药对土壤硝酸还原酶活性的影响表现为先抑制后激活的趋势,最大抑制率和激活率可达98.6%、580%。兽药对土壤过氧化氢酶活性的影响主要以激活作用为主,对土壤磷酸酶活性的影响则呈现＂激活-抑制＂的循环趋势。兽药对土壤脲酶活性的影响表现为,培养前期低浓度时激活,高浓度时抑制;培养后期低、高浓度时均抑制。兽药对土壤多酚氧化酶活性的影响表现为,培养前期激活,培养后期抑制。     

Interactive effect of dissolved organic matter and phenanthrene on soil enzymatic activities

The investigation of dissolved organic matter (DOM) on urease, catalase and polyphenol oxidase activity in a phenanthrene (Phe)-contaminated soil was conducted under laboratory incubation conditions. Values of soil enzymatic activity depended mainly on incubation time. In the initial 16 days, urease activity increased, and was followed by a decrease. In the initial 8 days, catalase activity decreased and then increased. Variation of polyphenol oxidase activity was just the reverse of catalase activity. After 30 days of incubation, no pronounced difference among treatments with Phe, Phe and DOM, and control were detected in urease, catalase and polyphenol oxidase activity. Phe might inhibit urease and catalase, and stimulate polyphenol oxidase. DOM could improve inhibition of Phe in soil urease and catalase activity during the initial period of applying DOM. Nevertheless, DOM had no significant effect on polyphenol oxidase activity in the Phe contaminated soil. There was a negative correlation between catalase and polyphenol oxidase (r = -0.761~(***)), and catalase and urease (r = -0.554~(**)). Additionally, a positive correlation between polyphenol oxidase and urease was also detected (r = 0.701~(***)). It is implied that the formed DOM after application of organic wastes into soils may counteract the inhibition of polycyclic aromatic hydrocarbons in soil enzyme activities.     

Effects of insoluble Zn, Cd, and EDTA on the growth, activities of antioxidant enzymes and uptake of Zn and Cd in Vetiveria zizanioides

A root-bag experiment was conducted to study the effects of insoluble Zn, Cd and ethylenediaminetetraacetic acid (EDTA) on the plant growth, activities of antioxidant enzymes, proline, glutathione (GSH), water-soluble proteins and malondialdehyde (MDA) of Vetiveria zizanioides, and its uptake capacity of Zn and Cd.The results showed that plant growth of V.zizanioides was inhibited by Zn and Cd.The shoot dry weight (SDW) and root dry weight (RDW) decrease by 0.3%, 8.0%, 9.4% and 10.4%, 15.1%, 24.2% compared to the control without EDTA addition, respectively.After adding EDTA, shoot and root dry weight decreased over 10% and 15% compared to results in the absence of EDTA, respectively.The toxicity from insoluble Zn and Cd in soil on SDW and RDW of V.zizanioides was in order: Zn+Cd > Cd > Zn.The activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), and contents of MDA and proline significantly increased, while the contents of GSH and water-soluble proteins markedly decreased with increasing Zn and Cd toxicity.With EDTA, shoot and root Zn concentrations increased in the Zn treatment by 7.3% and 37.4% compared to the plants grown in absence of EDTA.Shoot and root Cd concentrations in the combined Zn and Cd treatment with EDTA increased by 18.6% and 391.9% compared to the treatment without EDTA.However, Zn and Cd concentrations in shoot and roots decreased in the Cd treatment compared to the plants grown in absence of EDTA, with exception of root Cd concentration in the presence of EDTA).     

The effects of exogenous salicylic acid on growth and H2O2-metabolizing enzymes in rice seedlings under lead stress

Salicylic acid （SA） was an essential component of the plant resistance to pathogens and also plays an important role in mediating plant response to some abiotic stress. The possible effects of SA on the growth and H2O2-metabolizing enzymes in rice seedlings under lead stress were studied. When rice seedlings grown in nutrient solution containing Pb^2＋ （0, 0.05, 0.15, 0.25 mmol/L） for 18 d, the plant biomass as well as the chlorophyll content of leaves decreased with increasing Pb concentration. The pre-treatment with SA （treated with 0.1 mmol/L SA for 48 h before Pb stress） partially protected seedlings from Pb toxicity. The chlorophyll contents were significant higher in leaves of Pb-exposed with SA pre-treatment seedlings than in Pb-exposed plants at the same Pb intensity. SA pre-treated alone could significantly increase the length of shoot and root of seedlings but the vigour difference was not marked under long-term exposure to Pb toxicity. SA pre-treated influence the H2O2 level in leaves of seedlings by up-regulating the activity of superoxide dismutase （SOD）, repressing the activity of catalase （CAT） and ascorbate peroxidase （APX） depending on the concentrations of Pb^2＋ in the growth medium. The results supported the conclusion that SA played a positive role in rice seedlings against Pb toxicity.     

亚砷酸钠对酵母细胞抗氧化酶活性和脂质过氧化的影响

以模式生物酿酒酵母为材料,研究亚砷酸钠对细胞生长、抗氧化酶活性、丙二醛(MDA)含量及胞内活性氧(ROS)水平的影响。结果显示,加入亚砷酸钠(终浓度0.1~0.6 mmol·L~(-1))后,培养液在600 nm处的光密度值(OD600值)低于对照组,并呈浓度依赖性降低。经亚砷酸钠处理12 h后,酵母细胞中过氧化物酶(POD)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)和总抗氧化能力(T-AOC)活性均增高,但胞内ROS水平和MDA含量与对照组无显著差异。砷处理24 h后,POD在0.2 mmol·L~(-1)砷处理组中活性最高,而CAT、SOD和T-AOC活性呈浓度依赖性增高;胞内ROS水平和MDA含量在高浓度砷组(0.4和0.6 mmol·L~(-1))显著增高。结果表明,亚砷酸钠可抑制酵母细胞生长,改变细胞内抗氧化酶活性,较高浓度时可引起细胞氧化损伤。     

硝酸铊对浮萍(Lemna gibba L.)的生长抑制及其氧自由基损伤作用

为了探讨硝酸铊(Tl(I)-nitrate)对浮萍(Lemna gibba L.)的生长抑制作用及其可能的氧化损伤机制,设置了Tl(I)-nitrate的8个处理组(0.005、0.01、0.02、0.04、0.08、0.1、0.5和1.0 mg·L-1)和对照组(0.0 mg·L-1),进行96 h急性毒性实验,测定96 h内超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性及丙二醛含量。结果表明:96 h暴露时间下,浮萍生长受抑制程度与Tl(I)浓度之间呈正相关,Tl(I)-nitrate对浮萍的96 h EC50为0.076 mg·L-1,NOEC为0.01 mg·L-1。CAT活性随着Tl(I)-nitrate浓度升高逐渐降低,在0.5和1 mg·L-1时,有极显著差异(p0.01)产生,SOD活性在0.1 mg·L-1时显著升高(46%),POD活性和MDA含量在Tl(I)浓度0.5 mg·L-1时明显上升。当Tl(I)-nitrate胁迫超出浮萍抗氧化酶系统清除活性氧的能力时,活性氧积累导致浮萍受到不可逆转的氧化损伤。Tl(I)-nitrate对浮萍生长产生明显的抑制作用     

Smokeless tobacco extract impairs iron homeostasis in rats and human hepatoma,HepG2 cells

Tobacco exposure may alter homeostasis of iron (Fe), one of the most abundant and essential transition metals in the body. In this study, the effect of aqueous extract of smokeless tobacco was evaluated on Fe homeostasis in rats and human hepatoma, HepG2 cells. Our findings suggested that tobacco consumption even at low doses impairs Fe homeostasis leading to Fe deficiency anemia. Significant alterations were noted with respect to hematological parameters and expression patterns of selected intestinal Fe-transporters, Fe-binding proteins, and Fe-regulatory hormone, hepcidin. Impairment in the hepatic and renal antioxidant defense system was also observed in the treated rats. Histopathological studies revealed cirrhosis of liver and goblet cell hyperplasia of small intestine. Further, analysis of hepcidin promoter and its expression along with ferritin (expression and ELISA) in HepG2 cells demonstrated an enhanced expression of both the genes resulting in sequestration of Fe in treated cells, thus indicating systemic Fe deficiency.